14 ECOLOGICAL GENETICS AND THE EVOLUTION OF TRACE ELEMENT HYPERACCUMULATION IN PLANTS A. Joseph Pollard, Keri L. Dandridge, and Edward M. Jhee CONTENTS Introduction Genetic Variability in Hyperaccumulation Sources of Variation in Populations Evolution Research on Genetics of Hyperaccumulation Genetic Conclusions Ecological Significance of Hyperaccumulation Hyperaccumulation as a Plant Defense Nondefensive Hypotheses Ecological and Evolutionary Conclusions Summary and Applied Conclusions Acknowledgments References INTRODUCTION Many authors have described the potential uses of phytoremediation technology, as well as the need to understand the factors that control plant uptake of trace elements in developing this technology (e.g., Baker et al., 1994a; Salt et al., 1995). Plants that sequester trace metals at extremely high concentrations (hyperaccumulators), will probably play some role in phytoremediation, whether it be direct use as phytoremediation crops, indirect sources of genes for bioengineering of phytoreme- diation crops, or even more indirect physiological models through which we increase our knowledge of basic uptake processes. While much attention is focused on the Copyright © 2000 by Taylor & Francis physiological mechanisms of metal accumulation and tolerance, relatively little is known about the genetic and ecological factors that have led to the evolution of hyperaccumulation in nature. This chapter will attempt to summarize the current state of knowledge regarding these aspects of hyperaccumulation, present some new and previously unpublished findings, and generate hypotheses that may be relevant to future studies. The central question we will address in this chapter is: Why do plants hyperac- cumulate? or more formally: What is the selective advantage of hyperaccumulation and what evolutionary and adaptive processes have led to the development of this trait? The wide geographic and taxonomic ranges over which hyperaccumulation occurs (Baker and Brooks, 1989) imply that it has not arisen randomly in a single lineage, but has evolved independently in several taxa and localities; thus, it is reasonable to investigate the selective force or forces that may have led to this evolution. Possible ecological advantages of hyperaccumulation were reviewed in an excellent paper by Boyd and Martens (1993). We will attempt to expand on their foundation by including recent findings that have arisen since the publication of their review and by including both genetic and ecological perspectives on evolution. The central paradigm of evolutionary ecology is that adaptation occurs primarily as a result of natural selection. This is a process whereby in a genetically variable population some individuals are more suited to their environment than others, and consequently reproduce more successfully and leave more offspring to future gen- erations. Those offspring are likely to inherit the features that made their parents successful; therefore, over time, the traits conferring fitness in that environment will become more common in the population. Thus, evolution is an interaction between genetic and ecological factors. Currently, the genetics and ecology of hyperaccumu- lation are both active subjects for research. GENETIC VARIABILITY IN HYPERACCUMULATION This book is intended to be read by specialists from a wide range of disciplines. Therefore, it may be appropriate to provide a brief general review of some basic ideas in population and quantitative genetics before proceeding to explore the genet- ics of hyperaccumulation in natural populations. Readers wishing more detailed background should consult one of the many general texts on this topic (e.g., Falconer, 1989; Briggs and Walters, 1984; Crow, 1986; Silvertown and Lovett Doust, 1993) which act as references for much of the discussion that follows. SOURCES OF VARIATION IN POPULATIONS Phenotypic differences among plants are consequences of both genetic variation and the modifications imposed by the particular environments in which individuals are growing. Variation may be either discrete or continuous. Discrete phenotypic classes generally result from genetic control by a small number of loci. Genetic studies of discrete variation are typically conducted using classical Mendelian and population genetics, in which specific allele and genotype frequencies are estimated. Such Copyright © 2000 by Taylor & Francis studies may employ very elaborate schemes analyzing the offspring of controlled crosses (see Chapter 13). A continuous spectrum of variation usually results from a polygenic system of inheritance, in which many loci affect the same trait. Because of the large number of genes involved, continuous variation is typically studied through the methods of quantitative genetics, which concentrate on phenotypic measurements rather than gene frequencies. This approach is particularly appropriate when environmental influences are large compared to the effect of any one gene. Quantitative geneticists use a variety of cultivation and breeding schemes to attempt to separate and quantify the genetic and environmental determinants of the phenotype. Total phenotypic variance (V P ) may be partitioned according to the equation: in which V G represents genetic variation and V E represents environmentally induced variation. In the second part of the equation, the genetic variation has been further subdivided into V A , additive variation, and V N , nonadditive variation. Additive genetic variation involves characteristics that are transmitted in a simple manner from parents to offspring. Nonadditive variation represents differences among indi- viduals caused by various genetic interactions such as dominance, epistasis, maternal effects, and genotype-by-environment interactions. Although the underlying causes of nonadditive variation are genetic, it results from complex interactions among genes and thus does not necessarily predict simple parent–offspring resemblance. It is often useful to estimate the relative contributions of genotype and environ- ment to the phenotype. This is done using a statistic called heritability, symbolized h 2 , which varies between zero and one. The ratio V G /V P , known as “broad-sense heritability,” reflects the fraction of the population’s variability that is caused geno- typically and, by extension, the probable fraction of an individual’s phenotype determined by its genes. The ratio V A /V P is termed “narrow-sense heritability.” Because of the definition of additive variation, narrow-sense heritability can be said to reflect the degree to which phenotypes are determined by the genes of parents (i.e., the importance of inheritance in controlling the phenotype). In either case, heritability is a characteristic of a particular population in a particular environmental setting. Heritability estimates made under uniform conditions will usually be higher than those measured in a variable environment, because of the decreased contribution of V E to the denominator, V P . EVOLUTION Evolution is defined as change-over time in the genetic makeup of a population. The population genetic models of the Hardy-Weinberg law describe the factors that can potentially change gene frequencies in a population and thus drive evolution. These include genetic drift in small populations; mutations; migration or gene flow; non-random mating, including inbreeding; and natural selection, or differential fit- ness as measured through reproductive success. Most of these factors are essentially VVV VV V PGE AN E =+= + () + Copyright © 2000 by Taylor & Francis random; only natural selection directs change in such a way that a population becomes more suited to its environment over time. Differences in fitness depend on the ecological interactions between particular phenotypes and particular environments. However, only the genetic component of the phenotype can be passed on to the next generation and thus affect the evolution of the population. Natural selection cannot operate on traits which have no genetic variation, and will operate slowly on traits for which phenotypic variation derives predominantly from the environment and only slightly from genes. This is expressed by the equation: which indicates that response to selection (R) is equal to the product of heritability times the intensity of selection (S). Low heritability thus can impede the response of the population to even strong selection pressures. Variability within a species can exist at many spatial scales, including differences between populations and differences among individuals within a population. Vari- ability within a local population is subject to natural selection, allowing the popu- lation to adapt to its local conditions. If two populations experience different envi- ronmental conditions, selection thus can result in evolutionary divergence between them. However, differences between populations could also result from random, nonselective factors such as genetic drift. R ESEARCH ON G ENETICS OF H YPERACCUMULATION The existence of phenotypic variation in shoot metal concentration within species of hyperaccumulators has been recognized in many studies. The majority of such work (e.g., Reeves and Brooks, 1983a,b; Reeves et al., 1983a,b; Reeves, 1988) has examined the metal content of plants collected in their native field sites and thus includes both genetic and environmental sources of variation. Especially in cases where herbarium specimens have been analyzed, the elemental content of the soil in which the plants were growing is usually unknown. There have now been several studies in which hyperaccumulating plants from more than one population have been compared for metal content after being grown from seed under uniform and controlled conditions. Perhaps through sheer coinci- dence, all these studies involve species of Thlaspi that have the potential to hyper- accumulate nickel and zinc, and perhaps cadmium. Investigations of T. goesingense (Reeves and Baker, 1984), T. montanum var. montanum (Boyd and Martens, 1998), and T. caerulescens (Baker et al., 1994a,b) all found few statistically significant differences between populations in their ability to hyperaccumulate. In a much broader survey of variability in hyperaccumulation, Lloyd-Thomas (1995) compared populations of T. caerulescens from sites in Britain, Belgium, and Spain using both soil and hydroponic media. He reported statistically significant differences between populations in their ability to hyperaccumulate zinc, nickel, and cadmium, as well as a number of other metals accumulated to lower concentrations. Other recent studies (Pollard and Baker, 1996; Chaney et al., 1997; Meerts and Van Isacker, 1997) Rh S=• 2 LA4113 ch14 frame Page 254 Saturday, August 14, 1999 11:13 AM Copyright © 2000 by Taylor & Francis also confirm the existence of interpopulation variability in metal uptake among plants grown from seed in a common environment. Thus, these recent studies imply that ability to hyperaccumulate is not a completely uniform property within a species, but differs from population to population. Most of the studies described above did not use methods that would allow calculation of genetic statistics such as heritability. However, within-population variability is of great importance to questions of evolution and natural selection. Pollard and Baker (1996) examined zinc hyperaccumulation in T. caerulescens from two populations on Zn/Pb mine spoil in central Britain. In order to assess genetic trends, seeds were collected as sib families, i.e., as sets of seeds from a common mother plant. The seeds were germinated and plants were grown hydroponically in nutrient solution containing 10 mg l -1 Zn. Statistically significant differences in zinc concentration were found between populations and among the sib families within one population. It was possible to estimate broad-sense heritability based on resem- blances among siblings. In the variable population (Black Rocks, Derbyshire, U.K.), variation in zinc accumulation had a heritability of 0.179. The character of shoot dry weight was also analyzed and found to show significant within-population variability, with h 2 = 0.382. These findings imply that significant genetic variation in ability to accumulate metals may exist at the within-population level. Recent work in our laboratory has extended the analysis of sib families to examine zinc and nickel hyperaccumulation in populations of T. caerulescens from a variety of soil types (Table 14.1). Seeds from five populations, collected as sib families, were germinated and grown hydroponically on nutrient solutions supple- mented with either 10 mg l -1 Zn or 0.5 mg l -1 Ni. Leaves were removed from plants for analysis by atomic absorption spectrometry. (Full details of methods will be described in a future journal publication.) We found statistically significant differ- ences between populations in ability to accumulate both metals. Genetic variation TABLE 14.1 Characteristics of Source Populations for Thlaspi caerulescens Seeds Used in Heritability Studies Population Location Description Soil Zn Leaf Zn Soil Ni Leaf Ni BD England Pb/Zn mine spoil 8714 43,090 50 11 HF Wales Pb/Zn mine spoil 35,200 47,601 44 1 CH England Alluvial deposit 2214 19,384 50 6 (downstream from Pb/Zn mines) PB Spain Serpentine outcrop 58 1198 2918 18,357 PE Spain Alpine pasture 158 7777 48 0 Note: Soil concentrations are total μg g -1 based on aqua regia digests. Leaf concentrations are μg g -1 dry weight from field-collected leaves. Copyright © 2000 by Taylor & Francis among families within populations, as reflected in heritability values significantly greater than zero, was found in three populations for zinc and in one population for nickel (Table 14.2). Of particular interest was the population growing on soil without high metal content, in the Picos de Europa of northern Spain. Plants in the field accumulated zinc concentrations that were below the 10,000 μg g -1 criterion for hyperaccumulation, but were nonetheless remarkable for plants growing on “normal” soil (Table 14.1). In the laboratory, plants from this population displayed strong ability to hyperaccumulate zinc and nickel, but they also harbored highly significant between-family variation in ability to accumulate both metals (Table 14.2). Com- parisons between T. caerulescens populations from metal-enriched soils in Belgium and populations from unmineralized sites in Luxembourg (Meerts and Van Isacker, 1997) have also demonstrated the existence of variation in hyperaccumulation, both between and within populations. GENETIC CONCLUSIONS It appears, at least in the genus Thlaspi, that genetic variation in the ability to hyperaccumulate metals is demonstrated both between populations and within pop- ulations. There have been no signs of large, discrete polymorphisms expressed in natural populations; rather, there appears to be continuous variation, as would be expected from polygenic inheritance. Such systems may be truly quantitative if many loci control production of a single gene product that behaves in a dosage-dependent manner. Alternatively, polygenic inheritance can involve genes independently con- trolling several different aspects of physiology, such as mobilization, uptake, loading, transport, unloading, and storage of metals. Polygenic inheritance may be an obstacle TABLE 14.2 Variation Between and Within Populations of Thlaspi caerulescens in Ability to Accumulate Metals Zinc Nickel Population Pop. Mean (μg g -1 dry wt.) h 2 Pop. Mean (μg g -1 dry wt.) h 2 BD 12,958 NS 1950 NS HF 20,149 0.36 743 NS CH 11,456 0.11 686 NS PB 15,413 NS 830 NS PE 21,351 0.82 1066 0.67 Note: Plants were grown in nutrient solution with addition of either 10 mg l -1 Zn or 0.5 mg l -1 Ni (as sulfates). Differences among population means were statistically significant for each metal, based on nested ANOVA. Estimates of broad-sense heritability (h 2 ) are reported for each metal, in populations where one-way ANOVA revealed significant differences between sib families (NS = not significant). Populations are described in Table 14.1. Copyright © 2000 by Taylor & Francis to those attempting to isolate and manipulate a “hyperaccumulation gene.” However, the results described above do not rule out the possibility that a major gene for hyperaccumulation exists, but is fixed throughout T. caerulescens, and thus displays no variability (unless interspecific hybrids were generated; cf. Chapter 13). In such a situation, the variation expressed in natural populations could result from multiple modifier genes that might accompany the major gene. In an applied sense, the importance of the heritability values described above stems from the relationship between intensity of selection and response to selection (R = h 2 •S). The presence of a reservoir of variation with significant heritability implies that attempts to improve metal accumulation in potential phytoremediation crops through artificial selection may be fruitful. Pollard and Baker (1996) found no evidence for a trade-off between plant size and metal concentration, which might limit selection on total metal yield. Recent results regarding populations of hyper- accumulators from nonmetalliferous sites (Table 14.2, also Meerts and Van Isacker, 1997) suggest that such plants may be particularly valuable resources, because they may possess both a strong ability to accumulate metals (as a population average), and high levels of heritable variation that could indicate a potentially rapid response to selection for further increases in uptake. ECOLOGICAL SIGNIFICANCE OF HYPERACCUMULATION Reviewing the literature, Boyd and Martens (1993) grouped the published sugges- tions regarding the adaptive value of hyperaccumulation into five major hypotheses: (1) that hyperaccumulation functions to increase the metal tolerance of the plant, perhaps by aiding in the disposal of excess metals; (2) that hyperaccumulation increases the drought resistance of leaves; (3) that hyperaccumulation benefits plants through allelopathic interactions with other plants (e.g., creating a zone of toxic soil that suppresses competitors); (4) that hyperaccumulation is an inadvertent conse- quence of high-affinity uptake of other elements that may be scarce in mineralized substrates; and (5) that hyperaccumulation benefits plants through defense against herbivores or pathogens. In the years following their review, several investigations have supported the fifth hypothesis. HYPERACCUMULATION AS A PLANT DEFENSE Boyd and Martens (1994) showed that nickel hyperaccumulation in T. montanum var. montanum can be acutely toxic to larvae of Pieris rapae (Lepidoptera). Findings such as these are perhaps better described as antibiosis (an interaction that harms the herbivore), rather than as defense (an interaction that benefits the plant). As discussed by Pollard (1992), the two interactions are not necessarily synonymous. Martens and Boyd (1994) demonstrated that nickel hyperaccumulated by Strep- tanthus polygaloides causes similar acute antibiosis toward three species of insect herbivores. The same study also documented benefits to the plant (functional defense — Pollard, 1992) through deterrence of feeding in choice situations, resulting in greater plant growth and survival. Nickel also reduces bacterial and fungal growth, Copyright © 2000 by Taylor & Francis consequently improving plant growth and flowering in the same species (Boyd et al., 1994). Zinc hyperaccumulation can also have a deterrent role, as shown for insect and slug herbivory in T. caerulescens by Pollard and Baker (1997). The studies described in the preceding paragraph compared plants grown on high-metal vs. low-metal substrates; thus, they measured the response of herbivores to environmentally induced variation (V E ). In order to conclude that herbivore feeding pressures could select for the evolution of hyperaccumulation, it is necessary to show that herbivores discriminate in response to heritable genetic variation (V G ). In other words, to demonstrate that a feature of a plant represents an adaptation against herbivory, rather than an effective but coincidental defense evolved under selection by forces other than herbivory, requires the documentation of feeding deterrence in response to genetic variation that exists in nature (Jones, 1971; Pollard, 1992). We have recently approached this issue by using plants from our screening of genetic variation in zinc hyperaccumulation, as described earlier. The harvest of leaves for chemical analysis did not involve complete destruction of the plants. Thus, after characterizing the metal-accumulating ability of individuals grown in a common environment, we could subsequently use additional leaves for presentation to her- bivores. Leaves were removed from plants chosen to represent a contrast between high zinc accumulation and low zinc accumulation, in the common environment of culture solution with 10 mg L -1 Zn. Two contrasting leaves were placed in a 6-cm plastic petri dish. Across the whole experiment, the mean difference between the high-zinc and low-zinc leaves was 28,135 μg g -1 , and in no dish was the difference less than 20,000 μg g -1 . The area of each leaf was measured before the experiment using a digital leaf-area meter. The herbivore used for these experiments was the larva of P. napi oleracea (Lepidoptera, Pieridae), the veined white butterfly. This animal was chosen as a bioassay of palatability (Pollard and Baker, 1997), based on availability and will- ingness to eat T. caerulescens grown in low-zinc media. It is not known to feed on T. caerulescens in the wild, although Rocky Mountain populations do feed on the closely related T. montanum (on nonmetalliferous sites and thus containing low metal concentrations). Eggs (obtained from F. S. Chew at Tufts University) were allowed to hatch, and hatchlings were fed on radish leaves until large enough to be transferred to experimental dishes. One caterpillar was placed in each dish described above; 181 replicate trials were conducted. After 2 h of feeding, the remaining area of the leaves was measured, and leaf area consumed was determined by subtraction. Results of feeding trials are shown in Figure 14.1. Young larvae (less than 5 mm long) showed a slight preference for low-zinc leaves, but this difference was not statistically significant (paired t = 1.55, df = 62, p = 0.13). However, later-instar larvae showed very strong and significant preferences for the low-zinc leaves (paired t = 7.22, df = 117, p <0.001). Greater discrimination by later-instar larvae in choices among foodplant species was shown for P. napi larvae by Chew (1980). This appears to represent a behavioral reflection of the fact that larvae must eat immediately after hatching, and are able to become mobile foragers only during later instars. The same pattern was reflected Copyright © 2000 by Taylor & Francis here, in terms of intraspecific variation in leaf chemistry. Foodplant choices for young larvae might be made maternally through the oviposition preferences of adult females. However, Martens and Boyd (1994) could not find evidence that P. rapae oviposition was influenced by nickel content of S. polygaloides. These results confirm, using genetic variation in a common environment, the conclusion of previous herbivory studies using environmentally induced variation: that hyperaccumulation of metals in plants could have evolved under selection pressure from herbivores. Future studies will need to address the ability of herbivores to discriminate among even more subtle differences among phenotypes, especially if variation in metal accumulation ability is shown to be polygenic. However, it is important to note that phenotypic differences in metal concentration of the magnitude used in these experiments do occur within populations, both in the field and in controlled conditions (Lloyd-Thomas, 1995; Dandridge and Pollard, unpublished). NONDEFENSIVE HYPOTHESES Of the five hypotheses on the adaptive role of hyperaccumulation listed above, only the defensive hypothesis has received direct experimental study since the review of Boyd and Martens (1993). The drought-tolerance and allelopathic hypotheses remain relatively unexplored, although Boyd and Martens (1998) have recently argued in favor of the inadvertent uptake hypothesis. The idea that hyperaccumulation is a mechanism to provide metal tolerance remains pervasive. Krämer et al. (1996) demonstrated at a physiological level that free histidine plays a role in both metal accumulation and metal tolerance in Alyssum FIGURE 14.1 Leaf area of Thlaspi caerulescens consumed by Pieris napi larvae. All plants were grown in nutrient solution with 10 mg L -1 Zn. High-Zn and low-Zn plants were chosen based on prior chemical analysis of Zn content. In petri dish feeding trials, caterpillars were presented a choice between a high-Zn and low-Zn leaf. Mean leaf area consumed (±SE) is shown for early-instar larvae (N = 63) and late-instar larvae (N = 118). Copyright © 2000 by Taylor & Francis species. On the other hand, studies of variation in natural populations do not support the existence of a clear linkage between hyperaccumulation and tolerance. We will discuss this by examining correlations between soil metal concentration, plant tol- erance, and hyperaccumulation. It is well established for nonhyperaccumulators that tolerance can evolve in populations under the localized selective pressure of toxic soil (Antonovics et al., 1971). Thus, for these plants, a positive correlation exists between soil metal con- centration and tolerance in that nonmetalliferous soils bear populations with low metal tolerance (on average), while metal-contaminated sites support tolerant ecotypes. It is less clear whether this trend of correlation exists among the tolerant populations (i.e., whether the most toxic soils tend to bear the most tolerant popu- lations), but limited data seem to support such a trend (Gregory and Bradshaw, 1965). Hyperaccumulating taxa are generally metal-tolerant (Baker et al., 1994b; Krämer et al., 1996; Homer et al., 1991); however, there is also variation in tolerance among populations (Baker et al., 1994b; Lloyd-Thomas, 1995). Ingrouille and Smirnoff (1986) reported significant positive correlation between zinc concentrations in the soil and zinc tolerance in T. caerulescens in Britain, a conclusion which has been recently substantiated for the same species in continental Europe (Meerts and Van Isacker, 1997). A common feature of these studies was that they included plants from populations on nonmetalliferous soils. If hyperaccumulation represents a mechanism of metal tolerance, then we would expect relative ability to hyperaccumulate (based on studies in a uniform environ- ment) to be positively correlated with both soil toxicity and plant tolerance. The few data sets in which this analysis is possible (Lloyd-Thomas, 1995; Meerts and Van Isacker, 1997; Dandridge and Pollard, unpublished) consistently fail to support this prediction for the case of zinc in T. caerulescens. No positive correlations were detected, either between soil concentration and hyperaccumulation ability or between degree of tolerance and hyperaccumulation ability. All included populations from nonmetalliferous (thus, nontoxic) soils; these plants not only had the ability to hyperaccumulate, but did so more strongly than populations from zinc-mine spoil and other contaminated areas. Curiously, the data of Lloyd-Thomas (1995) do show a significant correlation between nickel tolerance and the ability to accumulate nickel in T. caerulescens across a range of populations mostly collected from zinc-mine spoil. The importance of this finding for a species that only rarely occurs on high-nickel substrates like serpentine remains to be investigated. Working with North American T. montanum var. montanum, which occurs both on serpentine and on normal soils, Boyd and Martens (1998) found no significant differences in the ability of serpentine and nonserpentine populations to take up nickel from uniform soil media (tolerance was not measured directly in their study). ECOLOGICAL AND EVOLUTIONARY CONCLUSIONS There is mounting support for the hypothesis that hyperaccumulation may have direct benefits for the plant, especially protection against herbivores and pathogens. The finding that plants from low-zinc soils possess strong powers of zinc accumu- Copyright © 2000 by Taylor & Francis [...]... U.K., 1989 Gregory, R.P.G and A.D Bradshaw Heavy metal tolerance in populations of Agrostis tenuis Sibth and other grasses New Phytol 64, 13 1-1 43, 1965 Homer, F.A., R.S Morrison, R.R Brooks, J Clemmens, and R.D Reeves Comparative studies of nickel, cobalt and copper uptake by some nickel hyperaccumulators of the genus Alyssum Plant Soil 138, 19 5-2 05, 1991 Ingrouille, M.J and N Smirnoff Thlaspi caerulescens... serpentine and nonserpentine populations of Thlaspi goesingense Hálácsy (Cruciferae) New Phytol 98, 19 1-2 04, 1984 Reeves, R.D and R.R Brooks European species of Thlaspi L (Cruciferae) as indicators of nickel and zinc J Geochem Explor 18, 27 5-2 83, 1983a Reeves, R.D and R.R Brooks Hyperaccumulation of lead and zinc by two metallophytes from mining areas of central Europe Environ Pollut (Ser A) 31, 27 7-2 85,... tolerance and accumulation in the metallicolous and non-metallicolous populations of Thlaspi caerulescens from continental Europe Plant Ecol 133, 22 1-2 31, 1997 Pollard, A.J The importance of deterrence: responses of grazing animals to plant variation, in Plant Resistance to Herbivores and Pathogens, Fritz, R.S and E.L Simms, Eds University of Chicago Press, Chicago, 21 6-2 39, 1992 Pollard, A.J and A.J.M... genetics of zinc hyperaccumulation in Thlaspi caerulescens New Phytol 132, 11 3-1 18, 1996 Pollard, A.J and A.J.M Baker Deterrence of herbivory by zinc hyperaccumulation in Thlaspi caerulescens (Brassicaceae) New Phytol 135, 65 5-6 58, 1997 Reeves, R.D Nickel and zinc accumulation by species of Thlaspi L., Cochlearia L., and other genera of the Brassicaceae Taxon 37, 30 9-3 18, 1988 Reeves, R.D and A.J.M... situ heavy metal decontamination of polluted soils using crops of metal-accumulating plants Res Conserv Recyc 11, 4 1-4 9,1994a Baker, A.J.M., R.D Reeves, and A.S.M Hajar Heavy metal accumulation and tolerance in British populations of the metallophyte Thlaspi caerulescens J & C Presl (Brassicaceae) New Phytol 127, 6 1-6 8, 1994b Baker, A.J.M and P.L Walker Ecophysiology of metal uptake by tolerant plants,... Brooks, and T.R Dudley Uptake of nickel by species of Alyssum, Bornmuellera, and other genera of old world tribus alysseae Taxon 32, 18 4-1 92, 1983a Copyright © 2000 by Taylor & Francis Reeves, R.D., R.M Macfarlane, and R.R Brooks Accumulation of nickel and zinc by western North American genera containing serpentine-tolerant species Am J Bot 70, 12971303, 1983b Salt, D.E., M Blaylock, P.B.A Nanda Kumar,... Malik, Y.M Li, S.L Brown, E.P Brewer, J.S Angle, and A.J.M Baker Phytoremediation of soil metals Curr Opin Biotechnol 8, 27 9-2 84, 1997 Chew, F.S Foodplant preferences of Pieris caterpillars (Lepidoptera) Oecologia 46, 34 7-3 53, 1980 Crow, J.F Basic Concepts in Population, Quantitative, and Evolutionary Genetics W.H Freeman, New York, 1986 Dandridge, K.L and A.J Pollard, unpublished data, 1996 Falconer,... hybridization, and genetic engineering (see Genetic Conclusions above) Genetic polymorphisms can also be useful tools for understanding the regulation of plant physiology Knowledge of the ecological role of hyperaccumulation in natural populations will be relevant in attempts to plant monocultures of metal-accumulating crops for phytoremediation Apart from these benefits to phytoremediation research, study of. .. FL, 15 5-1 77, 1990 Boyd, R.S and S.N Martens The raison d’être for metal hyperaccumulation by plants, in The Vegetation of Ultramafic (Serpentine) Soils, Baker, A.J.M., J Proctor, and R D Reeves, Eds Intercept, Andover, U.K., 27 9-2 89, 1993 Boyd, R.S and S.N Martens Nickel hyperaccumulated by Thlaspi montanum var montanum is acutely toxic to an insect herbivore Oikos 70, 2 1-2 5, 1994 Boyd, R.S and S.N... Bradshaw, and R.G Turner Heavy metal tolerance in plants Adv Ecol Res 7, 1-8 5, 1971 Baker, A.J.M Metal tolerance New Phytol 106 (Suppl.), 9 3-1 11, 1987 Baker, A.J.M and R.R Brooks Terrestrial higher plants which hyperaccumulate metallic elements — a review of their distribution, ecology, and phytochemistry Biorecovery 1, 8 1-1 26, 1989 Baker, A.J.M., S.P McGrath, C.M.D Sidoli, and R.D Reeves The possibility of . mg L -1 Zn. Two contrasting leaves were placed in a 6-cm plastic petri dish. Across the whole experiment, the mean difference between the high-zinc and low-zinc leaves was 28,135 μg g -1 , and. accumulation and metal tolerance in Alyssum FIGURE 14. 1 Leaf area of Thlaspi caerulescens consumed by Pieris napi larvae. All plants were grown in nutrient solution with 10 mg L -1 Zn. High-Zn and low-Zn. decontamination of polluted soils using crops of metal-accumulating plants. Res. Conserv. Recyc. 11, 4 1-4 9,1994a. Baker, A.J.M., R.D. Reeves, and A.S.M. Hajar. Heavy metal accumulation and tolerance